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空肠胃肠道间质瘤:大量胃肠道出血的罕见病因

Jejunal Gastrointestinal Stromal Tumor: A Strange Cause of Massive Gastrointestinal Bleeding.

作者信息

Martins Daniela, Costa Pedro, Guidi Gonçalo, Pinheiro Pedro, Pinto-de-Sousa João A

机构信息

General Surgery, Centro Hospitalar de Trás-Os-Montes e Alto Douro, Vila Real, PRT.

出版信息

Cureus. 2023 Aug 9;15(8):e43229. doi: 10.7759/cureus.43229. eCollection 2023 Aug.

Abstract

Jejunal gastrointestinal stromal tumors (GIST) are rare mesenchymal tumors of the gastrointestinal (GI) tract and a rare cause of massive GI bleeding. Due to this rarity and non-specific presentation, diagnosis and treatment may be difficult and often delayed. Urgent surgical intervention is crucial for controlling the source of bleeding and total tumor excision. Herein, we present the case of a 40-year-old male who presented to the emergency room (ER) with features of upper GI bleeding. He referred astheny and black stools, and was pale, sweaty, and tachycardic despite normal blood pressure. Rectal examination revealed melena, and laboratory findings revealed decreased hemoglobin (Hb) and elevated blood urea. Upper endoscopy was normal, and the Hb level dropped again to 6.9 g/dL; therefore, blood transfusion was required during ER observation. For further investigation, the patient underwent an angio-computed tomography scan, which revealed a lesion located in a jejunal loop as the probable bleeding source. Emergency exploratory laparotomy revealed a jejunal loop tumor. Segmental enterectomy containing the tumor was performed and the post-operative period was uneventful. The anatomopathological examination was compatible with low-risk GIST, and the multidisciplinary board agreed that surveillance was the best ongoing treatment. Due to the rarity of jejunal GIST as the cause of massive GI bleeding, diagnosis may be challenging, delaying prompt treatment with bleeding source control. In such cases, surgery may be both lifesaving and curative. Therefore, these tumors should not be forgotten when managing patients with occult GI bleeding with an atypical presentation to prevent delays in treatment and severe outcomes.

摘要

空肠胃肠道间质瘤(GIST)是胃肠道罕见的间叶性肿瘤,也是导致大量胃肠道出血的罕见原因。由于其罕见性和非特异性表现,诊断和治疗可能会很困难,而且常常延迟。紧急手术干预对于控制出血源和完整切除肿瘤至关重要。在此,我们报告一例40岁男性患者,他因上消化道出血症状就诊于急诊室。他自述乏力和黑便,尽管血压正常,但面色苍白、多汗且心动过速。直肠检查发现有黑便,实验室检查结果显示血红蛋白(Hb)降低,血尿素升高。上消化道内镜检查正常,Hb水平再次降至6.9 g/dL;因此,在急诊观察期间需要输血。为了进一步检查,患者接受了血管计算机断层扫描,结果显示位于空肠袢的一个病变可能是出血源。急诊剖腹探查发现一个空肠袢肿瘤。进行了包含肿瘤的节段性肠切除术,术后恢复顺利。解剖病理学检查结果与低风险GIST相符,多学科团队一致认为监测是最佳的后续治疗方案。由于空肠胃肠道间质瘤作为大量胃肠道出血原因的罕见性,诊断可能具有挑战性,会延误对出血源的及时控制治疗。在这种情况下,手术可能既挽救生命又能治愈疾病。因此,在处理表现不典型的隐匿性胃肠道出血患者时,不应忽视这些肿瘤,以防止治疗延误和严重后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1d/10491460/d5ef3d326c3a/cureus-0015-00000043229-i01.jpg

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